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NM_001164277.2(SLC37A4):c.1176T>G (p.Ser392Arg) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 9, 2021
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV002550382.2

Allele description [Variation Report for NM_001164277.2(SLC37A4):c.1176T>G (p.Ser392Arg)]

NM_001164277.2(SLC37A4):c.1176T>G (p.Ser392Arg)

Gene:
SLC37A4:solute carrier family 37 member 4 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11q23.3
Genomic location:
Preferred name:
NM_001164277.2(SLC37A4):c.1176T>G (p.Ser392Arg)
HGVS:
  • NC_000011.10:g.119025024A>C
  • NG_013331.1:g.10882T>G
  • NM_001164277.2:c.1176T>GMANE SELECT
  • NM_001164278.2:c.1242T>G
  • NM_001164279.2:c.957T>G
  • NM_001164280.2:c.1176T>G
  • NM_001467.6:c.1176T>G
  • NP_001157749.1:p.Ser392Arg
  • NP_001157750.1:p.Ser414Arg
  • NP_001157751.1:p.Ser319Arg
  • NP_001157752.1:p.Ser392Arg
  • NP_001458.1:p.Ser392Arg
  • LRG_187:g.10882T>G
  • NC_000011.9:g.118895734A>C
  • NM_001467.5:c.1176T>G
Protein change:
S319R
Links:
dbSNP: rs782552989
NCBI 1000 Genomes Browser:
rs782552989
Molecular consequence:
  • NM_001164277.2:c.1176T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001164278.2:c.1242T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001164279.2:c.957T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001164280.2:c.1176T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001467.6:c.1176T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003732983Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Nov 9, 2021) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV003732983.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The c.1176T>G (p.S392R) alteration is located in exon 9 (coding exon 8) of the SLC37A4 gene. This alteration results from a T to G substitution at nucleotide position 1176, causing the serine (S) at amino acid position 392 to be replaced by an arginine (R). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024